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Dual-Modified Cellulose Nanofiber Membranes with Boosted Surface Charge for High-Performance Osmotic Energy
Xuejiao Lin1, Shenming Tao1, Xijun Wang1
1State Key Laboratory of Advanced Papermaking and Paper-based Materials, South China University of Technology, Guangzhou, China.
Small (Weinheim an Der Bergstrasse, Germany)
|April 9, 2026
Summary
Highly charged cellulose nanofiber membranes were developed for enhanced osmotic energy conversion. This dual-modification strategy significantly boosts power output and ion selectivity for sustainable energy solutions.
Area of Science:
- Materials Science
- Nanotechnology
- Renewable Energy
Background:
- Nanofluidics holds promise for osmotic energy conversion, but low nanomaterial surface charge limits membrane ion selectivity, permeability, and power output.
- Current single-step modification methods face substitution limits, hindering substantial surface charge achievement in membranes.
- Optimizing nanochannel structure alongside surface charge is crucial for efficient ion transport.
Purpose of the Study:
- To develop novel, oppositely charged cellulose nanofiber membranes with enhanced ion selectivity and permeability for osmotic energy conversion.
- To overcome the limitations of single-step modifications using a dual-modification strategy.
- To investigate the synergistic effects of enhanced surface charge and tailored nanochannels on membrane performance.
Main Methods:
- A dual-modification strategy involving small-molecule functionalization and polymer grafting was employed to create highly charged cellulose nanofiber membranes.
- Systematic investigation of the membranes' surface charge, nanochannel structure, and ion transport properties.
- Fabrication and testing of a reverse electrodialysis (RED) unit utilizing the developed membranes to assess power density and scalability.
Main Results:
- The dual-modified membranes exhibited significantly enhanced surface charge and optimized nanochannel structures, leading to improved ion selectivity (t_+ of 0.97).
- Negatively and positively charged membranes achieved power densities of 5.1 W·m⁻² and 4.6 W·m⁻², respectively, representing substantial improvements over pristine membranes.
- A RED unit with these membranes delivered a power density of 12.9 W·m⁻² (5/0.01 M) and generated 2.5 V with 15 membrane pairs, demonstrating practical scalability.
Conclusions:
- The proposed dual-modification strategy effectively enhances surface charge and maintains optimal nanochannel structure in cellulose nanofiber membranes.
- These engineered membranes exhibit superior ion selectivity and transport, leading to significantly boosted power output for osmotic energy conversion.
- The developed membranes offer a sustainable, low-cost, and scalable solution for efficient osmotic energy harvesting, advancing nanofluidic applications.

